Evans E A
Biophys J. 1985 Jul;48(1):175-83. doi: 10.1016/S0006-3495(85)83770-X.
The mechanics of membrane-membrane adhesion are developed for the approximation that the molecular cross-bridging forces are continuously distributed as a normal stress (force per unit area). The significance of the analysis is that the finite range of the cross-bridging forces and the microscopic contact angle are not assumed negligible. Since the cross-bridging and adhesion forces are finite range interactions, there are two membrane regions: a free zone where the membranes are not subject to attractive forces; and an adherent zone where the membranes are held together by attractive stresses. The membrane is treated as an elastic continuum. The approach is to analyze the mechanics for each zone separately and then to require continuity of the solutions at the interface between the zones. Final solution yields the membrane contour and stresses proximal to and within the contact zone as well as the microscopic contact angle at the edge of the contact zone. It is demonstrated that the classical Young equation is consistent with this model. The results show that the microscopic contact angle becomes appreciable when the strength of adhesion is large or the length of the cross-bridge is large; however, the microscopic contact angle approaches zero as the membrane elastic stiffness increases. The solution predicts the width of the contact zone over which molecular bonds are stretched. It is this boundary region where increased biochemical activity is expected. In the classical model presented here, the level of tension necessary to oppose spreading of the contact is equal to the minimal level of tension required to separate the adherent membranes. This behavior is in contrast with that derived for the case of discrete molecular cross-bridges where the possibility of different levels of tension associated with adhesion and separation is introduced. The discrete cross-bridge case is the subject of a companion paper.
针对分子交联力作为法向应力(单位面积上的力)连续分布的近似情况,推导了膜 - 膜粘附的力学原理。该分析的重要意义在于,未假定交联力的有限范围和微观接触角可忽略不计。由于交联力和粘附力是有限范围的相互作用,因此存在两个膜区域:一个是自由区域,膜在该区域不受吸引力作用;另一个是粘附区域,膜在该区域通过吸引力应力保持在一起。将膜视为弹性连续体。方法是分别分析每个区域的力学原理,然后要求在区域之间的界面处解具有连续性。最终解给出了接触区域近端和内部的膜轮廓和应力,以及接触区域边缘的微观接触角。结果表明,经典的杨氏方程与该模型一致。结果显示,当粘附强度大或交联长度大时,微观接触角变得明显;然而,随着膜的弹性刚度增加,微观接触角趋近于零。该解预测了分子键被拉伸的接触区域的宽度。正是在这个边界区域预期会有增强的生化活性。在此提出的经典模型中,抵抗接触扩展所需的张力水平等于分离粘附膜所需的最小张力水平。这种行为与离散分子交联情况所推导的行为形成对比,在离散分子交联情况下引入了与粘附和分离相关的不同张力水平的可能性。离散交联情况是一篇配套论文的主题。